Eligard 7.5 mg (Sanofi-Aventis)

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DESCRIPTION

ELIGARD ^® 7.5 mg is a sterile polymeric matrix formulation of leuprolide acetate for subcutaneous injection. It is designed to deliver 7.5 mg of leuprolide acetate at a controlled rate over a one month therapeutic period.

Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin releasing hormone (GnRH or LH-RH) that, when given continuously, inhibits pituitary gonadotropin secretion and suppresses testicular and ovarian steroidogenesis. The analog possesses greater potency than the natural hormone. The chemical name is 5-oxo-L-prolyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosyl-D-leucyl-L-leucyl-L-arginyl-N-ethyl-L-prolinamide acetate (salt) with the following structural formula:

ELIGARD ^® 7.5 mg is prefilled and supplied in two separate, sterile syringes whose contents are mixed immediately prior to administration. The two syringes are joined and the single dose product is mixed until it is homogenous. ELIGARD ^® 7.5 mg is administered subcutaneously where it forms a solid drug delivery depot.

One syringe contains the ATRIGEL ^® Delivery System and the other contains leuprolide acetate. The ATRIGEL ^® Delivery System is a polymeric (non-gelatin containing) delivery system consisting of a biodegradable poly(DL-lactide-co-glycolide) (PLGH) polymer formulation dissolved in a biocompatible solvent, N -methyl-2-pyrrolidone (NMP). PLGH is a co-polymer with a 50:50 molar ratio of DL-lactide to glycolide containing carboxyl end groups. The second syringe contains leuprolide acetate and the constituted product is designed to deliver 7.5 mg of leuprolide acetate at the time of subcutaneous injection.

ELIGARD ^® 7.5 mg delivers 7.5 mg of leuprolide acetate (equivalent to approximately 7.0 mg leuprolide free base) dissolved in 160 mg N -methyl-2-pyrrolidone and 82.5 mg poly(DL-lactide-co-glycolide). The approximate weight of the administered formulation is 250 mg.

CLINICAL PHARMACOLOGY

Leuprolide acetate, an LH-RH agonist, acts as a potent inhibitor of gonadotropin secretion when given continuously in therapeutic doses. Animal and human studies indicate that after an initial stimulation, chronic administration of leuprolide acetate results in suppression of ovarian and testicular steroidogenesis. This effect is reversible upon discontinuation of drug therapy.

In humans, administration of leuprolide acetate results in an initial increase in circulating levels of luteinizing hormone (LH) and follicle stimulating hormone (FSH), leading to a transient increase in levels of the gonadal steroids (testosterone and dihydrotestosterone in males, and estrone and estradiol in premenopausal females). However, continuous administration of leuprolide acetate results in decreased levels of LH and FSH. In males, testosterone is reduced to below castrate threshold (</= 50 ng/dL). These decreases occur within two to four weeks after initiation of treatment. Long-term studies have shown that continuation of therapy with leuprolide acetate maintains testosterone below the castrate level for up to seven years.

PHARMACODYNAMICS

Following the first dose of ELIGARD ^® 7.5 mg, mean serum testosterone concentrations transiently increased, then fell to below castrate threshold (</= 50 ng/dL) within three weeks (Figure 1). Continued monthly treatment maintained castrate testosterone suppression throughout the study. No breakthrough of testosterone concentrations above castrate threshold (> 50 ng/dL) occurred at any time during the study once castrate suppression was achieved.

Leuprolide acetate is not active when given orally.

PHARMACOKINETICS

Absorption:    The pharmacokinetics/pharmacodynamics observed during three once monthly injections (ELIGARD ^® 7.5 mg) in 20 patients with advanced carcinoma of the prostate is shown in Figure 1. Mean serum leuprolide concentrations following the initial injection rose to 25.3 ng/mL (C _max ) at approximately 5 hours after injection. After the initial increase following each injection, serum concentrations remained relatively constant (0.28 - 2.00 ng/mL). There was no evidence of significant accumulation during repeated dosing. Nondetectable leuprolide plasma concentrations have been observed during chronic ELIGARD ^® 7.5 mg administration, but testosterone levels were maintained at castrate levels.

Distribution:    The mean steady-state volume of distribution of leuprolide following intravenous bolus administration to healthy male volunteers was 27 L. ¹ In vitro binding to human plasma proteins ranged from 43% to 49%.

Metabolism:    In healthy male volunteers, a 1 mg bolus of leuprolide administered intravenously revealed that the mean systemic clearance was 8.34 L/h, with a terminal elimination half-life of approximately 3 hours based on a two compartment model. ¹

No drug metabolism study was conducted with ELIGARD ^® 7.5 mg. Upon administration with different leuprolide acetate formulations, the major metabolite of leuprolide acetate is a pentapeptide (M-1) metabolite.

Excretion:    No drug excretion study was conducted with ELIGARD ^® 7.5 mg.

Special Populations:

Geriatrics:    The majority (70%) of the 128 patients studied in these clinical trials were age 70 and older.

Pediatrics:    The safety and effectiveness of ELIGARD ^® 7.5 mg in pediatric patients have not been established (see CONTRAINDICATIONS ).

Race:    In patients studied (26 White, 2 Hispanic), mean serum leuprolide concentrations were similar.

Renal and Hepatic Insufficiency:    The pharmacokinetics of ELIGARD ^® 7.5 mg in hepatically and renally impaired patients have not been determined.

Drug-Drug Interactions:    No pharmacokinetic drug-drug interaction studies were conducted with ELIGARD ^® 7.5 mg.

CLINICAL STUDIES

In one open-label, multicenter study (AGL9904), 120 patients with advanced prostate cancer were treated with six monthly injections of ELIGARD ^® 7.5 mg. Eighty-nine patients had stage C disease and 31 patients had stage D disease. This study evaluated the achievement and maintenance of serum testosterone suppression over six months of therapy.

The mean testosterone concentration increased from 361.3 ng/dL at Baseline to 574.6 ng/dL at Day 3 following the initial subcutaneous injection. The mean serum testosterone concentration then decreased to below Baseline by Day 10 and was 21.8 ng/dL on Day 28. At the conclusion of the study (Month 6), mean testosterone concentration was 6.1 ng/dL (Figure 2).

Serum testosterone was suppressed to below the castrate threshold (</= 50 ng/dL) by Day 28 (Week 4) in 112 of 119 (94.1%) patients remaining in the study. The remaining seven patients all attained the castrate threshold by Day 42. Once testosterone suppression at or below serum concentrations of 50 ng/dL was achieved, no patients (0%) demonstrated breakthrough (concentration above 50 ng/dL) at any time in the study. All 117 evaluable patients in the study at Month 6 (two patients withdrew for reasons unrelated to drug) had testosterone concentrations of </= 50 ng/dL.

Serum PSA decreased in all patients whose Baseline values were elevated above the normal limit. Mean values were reduced 94% from Baseline to Month 6. At Month 6, PSA levels had decreased to within normal limits in 94% of patients who presented with elevated levels at Baseline.

Other secondary efficacy endpoints evaluated included WHO performance status, bone pain, urinary pain and urinary signs and symptoms. At Baseline, 88% of patients were classified as "fully active" by the WHO performance status scale (Status=0) and 11% as "restricted in strenuous activity but ambulatory and able to carry out work of a light or sedentary nature" (Status=1). These percentages were unchanged at Month 6. At Baseline, patients experienced little bone pain, with a mean score of 1.22 (range 1-9) on a scale of 1 (no pain) to 10 (worst pain possible). At Month 6, the mean bone pain score was essentially unchanged at 1.26 (range 1-7). Urinary pain, scored on the same scale, was similarly low, with a mean of 1.12 at Baseline (range 1-5) and 1.07 at Month 6 (range 1-8). Urinary signs and symptoms were similarly low at Baseline and decreased modestly at Month 6. In addition, there was a reduction in patients with prostate abnormalities detected during physical exam from 102 (85%) at Screening to 77 (64%) at Month 6.

INDICATIONS AND USAGE

ELIGARD ^® 7.5 mg is indicated for the palliative treatment of advanced prostate cancer.

CONTRAINDICATIONS

1. ELIGARD ^® 7.5 mg is contraindicated in patients with hypersensitivity to GnRH, GnRH agonist analogs or any of the components of ELIGARD ^® 7.5 mg. Anaphylactic reactions to synthetic GnRH or GnRH agonist analogs have been reported in the literature. ²
2. ELIGARD ^® 7.5 mg is contraindicated in women and in pediatric patients and was not studied in women or children. Moreover, leuprolide acetate can cause fetal harm when administered to a pregnant woman. Major fetal abnormalities were observed in rabbits but not in rats after administration of leuprolide acetate throughout gestation. There were increased fetal mortality and decreased fetal weights in rats and rabbits. The effects on fetal mortality are expected consequences of the alterations in hormonal levels brought about by this drug. The possibility exists that spontaneous abortion may occur.

WARNINGS

ELIGARD ^® 7.5 mg, like other LH-RH agonists, causes a transient increase in serum concentrations of testosterone during the first week of treatment. Patients may experience worsening of symptoms or onset of new signs and symptoms during the first few weeks of treatment, including bone pain, neuropathy, hematuria, or bladder outlet obstruction. Isolated cases of ureteral obstruction and/or spinal cord compression, which may contribute to paralysis with or without fatal complications, have been observed in the palliative treatment of advanced prostate cancer using LH-RH agonists (see PRECAUTIONS ).

If spinal cord compression or renal impairment develops, standard treatment of these complications should be instituted.

PRECAUTIONS

General:    Patients with metastatic vertebral lesions and/or with urinary tract obstruction should be closely observed during the first few weeks of therapy (see WARNINGS section).

Laboratory tests:    Response to ELIGARD ^® 7.5 mg should be monitored by measuring serum concentrations of testosterone and prostate-specific antigen periodically.

In the majority of patients, testosterone levels increased above Baseline during the first week, declining thereafter to Baseline levels or below by the end of the second week. Castrate levels were generally reached within two to four weeks and once achieved were maintained for the duration of treatment. No increases to above the castrate level occurred in any of the patients.

Results of testosterone determinations are dependent on assay methodology. It is advisable to be aware of the type and precision of the assay methodology to make appropriate clinical and therapeutic decisions.

Drug Interactions:    See PHARMACOKINETICS

Drug/Laboratory Test Interactions:    Therapy with leuprolide results in suppression of the pituitary-gonadal system. Results of diagnostic tests of pituitary gonadotropic and gonadal functions conducted during and after leuprolide therapy may be affected.

Carcinogenesis, Mutagenesis, Impairment of Fertility:    Two-year carcinogenicity studies were conducted with leuprolide acetate in rats and mice. In rats, a dose-related increase of benign pituitary hyperplasia and benign pituitary adenomas was noted at 24 months when the drug was administered subcutaneously at high daily doses (0.6 to 4 mg/kg). There was a significant but not dose-related increase of pancreatic islet-cell adenomas in females and of testicular interstitial cell adenomas in males (highest incidence in the low dose group). In mice, no leuprolide acetate-induced tumors or pituitary abnormalities were observed at a dose as high as 60 mg/kg for two years. Patients have been treated with leuprolide acetate for up to three years with doses as high as 10 mg/day and for two years with doses as high as 20 mg/day without demonstrable pituitary abnormalities. No carcinogenicity studies have been conducted with ELIGARD ^® 7.5 mg.

Mutagenicity studies have been performed with leuprolide acetate using bacterial and mammalian systems and with ELIGARD ^® 7.5 mg in bacterial systems. These studies provided no evidence of a mutagenic potential.

Pregnancy, Teratogenic Effects:    Pregnancy category X (See CONTRAINDICATIONS ).

Pediatric Use:    ELIGARD ^® 7.5 mg is contraindicated in pediatric patients and was not studied in children (see CONTRAINDICATIONS ).

ADVERSE REACTIONS

The safety of ELIGARD ^® 7.5 mg was evaluated in eight surgically castrated males and 120 patients with advanced prostate cancer in two clinical trials. ELIGARD ^® 7.5 mg, like other LH-RH analogs, caused a transient increase in serum testosterone concentrations during the first week of treatment. Therefore, potential exacerbations of signs and symptoms of the disease during the first few weeks of treatment are of concern in patients with vertebral metastases and/or urinary obstruction or hematuria. If these conditions are aggravated, it may lead to neurological problems such as weakness and/or paresthesia of the lower limbs or worsening of urinary symptoms (see WARNINGS and PRECAUTIONS ).

In Study AGL9904, 120 patients were dosed with ELIGARD ^® 7.5 mg for up to six months and injection sites were closely monitored. In all, 716 injections of ELIGARD ^® 7.5 mg were administered. Transient burning/stinging was reported following 248 (34.6%) injections, with the majority (84%) of these events reported as mild. Pain was reported following 4.3% of study injections (18.3% of patients) and was generally reported as brief in duration and mild in intensity.

Erythema was reported following 2.6% of injections (12.5% of patients). These events were all reported as mild and generally resolved within a few days post-injection. Mild bruising was reported following 2.5% of injections (11.7% of patients). Pruritis, induration, and ulceration was reported following 1.4% (11 patients), 0.4% (3 patients), and 0.1% (1 patient) of study injections, respectively.

These localized adverse events were non-recurrent over time. No patient discontinued therapy due to an injection site adverse event.

The following possibly or probably related systemic adverse events occurred during clinical trials of up to six months of treatment with ELIGARD ^® 7.5 mg, and were reported in >/= 2% of patients (Tables 1 and 2). Often, causality is difficult to assess in patients with metastatic prostate cancer. Reactions considered not drug-related are excluded.

In addition, the following possibly or probably related systemic adverse events were reported by < 2% of the patients using ELIGARD ^® 7.5 mg in clinical studies.

General:   Sweating, insomnia, syncope

Gastrointestinal:   Flatulence, constipation

Hematologic:   Decreased red blood cell count, hematocrit and hemoglobin

Metabolic:   Weight gain

Musculoskeletal:   Tremor, backache, joint pain

Nervous:   Disturbance of smell and taste, depression, vertigo

Skin:   Alopecia

Urogenital:   Testicular soreness, impotence * , decreased libido * , gynecomastia, breast soreness

Changes in Bone Density:    Decreased bone density has been reported in the medical literature in men who have had orchiectomy or who have been treated with an LH-RH agonist analog. ³ It can be anticipated that long periods of medical castration in men will have effects on bone density.

OVERDOSAGE

In clinical trials using daily subcutaneous leuprolide acetate in patients with prostate cancer, doses as high as 20 mg/day for up to two years caused no adverse effects differing from those observed with the 1 mg/day dose.

DOSAGE AND ADMINISTRATION

The recommended dose of ELIGARD ^® 7.5 mg is one injection every month. The injection delivers 7.5 mg of leuprolide acetate, incorporated in a polymer formulation. It is administered subcutaneously and provides continuous release of leuprolide for one month.

Once mixed, ELIGARD ^® 7.5 mg should be discarded if not administered within 30 minutes.

As with other drugs administered by subcutaneous injection, the injection site should vary periodically. The specific injection location chosen should be an area with sufficient soft or loose subcutaneous tissue. In clinical trials, the injection was administered in the upper- or mid-abdominal area. Avoid areas with brawny or fibrous subcutaneous tissue or locations that could be rubbed or compressed (i.e., with a belt or clothing waistband).

Mixing and Administration Procedure

IMPORTANT:    Allow the product to reach room temperature before using. Once mixed, the product must be administered within 30 minutes.

Follow the instructions as directed to ensure proper preparation of ELIGARD ^® 7.5 mg prior to administration:

ELIGARD ^® 7.5 mg is packaged in a pouch that contains two smaller pouches (Figure 3), a needle cartridge and a desiccant pack (Figure 4). Syringe A pouch contains the sterile Syringe A pre-filled with the ATRIGEL ^® polymer system and a long white replacement plunger rod (Figure 5). Syringe B pouch contains the sterile Syringe B pre-filled with leuprolide acetate powder (Figure 6).

1. On a clean field, open all of the pouches and remove the contents. Discard the desiccant pack.
     
     
2. Pull out the blue-tipped short plunger rod and attached stopper from Syringe B and discard (Figure 7). Gently insert the long, white replacement plunger rod into the gray primary stopper remaining in Syringe B by twisting it in place (Figure 8).
     
     
3. Unscrew the clear cap from Syringe A (Figure 9). Remove the gray rubber cap from Syringe B (Figure 10).
     
4. Join the two syringes together by pushing in and twisting until secure (Figure 11).
     
5. Inject the liquid contents of Syringe A into Syringe B containing the leuprolide acetate. Thoroughly mix the product by pushing the contents of both syringes back and forth between syringes (approximately 45 seconds) to obtain a uniform suspension (Figure 12). When thoroughly mixed, the suspension will appear a light tan to tan color. Please note: Product must be mixed as described; shaking will not provide adequate mixing of the product.
     
6. Hold the syringes vertically with Syringe B on the bottom. The syringes should remain securely coupled. Draw the entire mixed product into Syringe B (short, wide syringe) by depressing the Syringe A plunger and slightly withdrawing the Syringe B plunger. Uncouple Syringe A while continuing to push down on the Syringe A plunger (Figure 13). Please note: Small air bubbles will remain in the formulation--this is acceptable.
     
     
     
7. Hold Syringe B upright. Remove the pink cap on the bottom of the sterile needle cartridge by twisting it (Figure 14). Attach the needle cartridge to the end of Syringe B (Figure 15) by pushing in and turning the needle until it is firmly seated. Do not twist the needle onto the syringe until it is stripped. Pull off the clear needle cartridge cover prior to administration (Figure 16).
8. Choose an injection site on the abdomen, upper buttocks, or anywhere with adequate amounts of subcutaneous tissue that does not have excessive pigment, nodules, lesions, or hair. Since you can vary the injection site with a subcutaneous injection, choose an area that hasn't recently been used.
9. Cleanse the injection-site area with an alcohol swab. ⁴
     
10. Using the thumb and forefinger of your nondominant hand, grab and bunch the area of skin around the injection site. ⁴
      
11. Using your dominant hand, insert the needle quickly. The approximate angle you use will depend on the amount and fullness of the subcutaneous tissue and the length of the needle. ⁴
      
12. After the needle is inserted, release the skin with your nondominant hand. ⁴
13. Inject the drug using a slow, steady push. Press down on the plunger until the syringe is empty. ⁴
14. Withdraw the needle quickly at the same angle used for insertion. ⁴
15. Gently massage the injection area with a cotton ball or gauze pad. ⁴
16. Discard all components safely in an appropriate biohazard container.
17. Remove your gloves and wash your hands. Document both the procedure and the patient's response to the injection.

HOW SUPPLIED

ELIGARD ^® 7.5 mg is available in a single use kit. The kit consists of a two-syringe mixing system, a 20-gauge half-inch needle, a silicone desiccant pouch to control moisture uptake, and package insert for constitution and administration procedures. Each syringe is individually packaged. One contains the ATRIGEL ^® Delivery System and the other contains leuprolide acetate. When constituted, ELIGARD ^® 7.5 mg is administered as a single dose.

(NDC 0024-0793-75)

Rx only

Store at 2-8 °C (36-46 °F)

Sanofi-Synthelabo

Manufactured for Sanofi-Synthelabo Inc.

New York, NY 10016

by Atrix Laboratories, Inc.

Fort Collins, CO 80525

1 Sennello LT et al. Single-dose pharmacokinetics of leuprolide in humans following intravenous and subcutaneous administration. J Pharm Sci 1986; 75(2): 158-160.

2 MacLeod TL et. al. Anaphylactic reaction to synthetic luteinizing hormone releasing hormone. Fertil Steril 1987 Sept; 48(3): 500-502.

3 Hatano T et. al. Incidence of bone fracture in patients receiving luteinizing hormone-releasing hormone agonists for prostate cancer. BJU International 2000 86: 449-452.

4 National Institutes of Health. Giving a subcutaneous injection. Bethesda, MD; 2002.

04295 Rev 5 7/03 Revised July 2003

Copyright, Sanofi-Synthelabo Inc. 1996, 2003

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